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Reversible Dehydrogenation of Magnesium Borohydride to Magnesium Triborane in the Solid State Under Moderate Conditions

Journal Article · · Chemical Communications, 47(4):1330-1332
DOI:https://doi.org/10.1039/C0CC03461D· OSTI ID:1006285
Thermal decomposition of magnesium borohydride, Mg(BH4)2, in the solid state was studied by a combination of PCT, TGA/MS and NMR spectroscopy. Dehydrogenation of Mg(BH4)2 at 200 °C, results in the highly selective formation of magnesium triborane, Mg(B3H8)2. This process is reversible at 250 °C under 120 atm H2. Dehydrogenation at higher temperature, > 300 °C, produces a complex mixture of polyborane species. Solution phase 11B NMR spectra of the hydrolyzed decomposition products reveals the formation of the B3H8 anion, boric acid from hydrolysis of the unstable polyboranes (BnHx) (n = 3-11, x >8), and the closoborane B12H12 dianion as a minor product. A BH condensation mechanism involving metal hydride formation is proposed to explain the limited reversible hydrogen storage in magnesium borohydride.
Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
1006285
Report Number(s):
PNNL-SA-74978; 25661; EB4202000
Journal Information:
Chemical Communications, 47(4):1330-1332, Journal Name: Chemical Communications, 47(4):1330-1332 Journal Issue: 4 Vol. 47
Country of Publication:
United States
Language:
English

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